Comparative aspects of the brain growth spurt

Quantitative growth and development of human brain

Dobbing, J., & Sands, J. (1973) · Archives of Disease in Childhood · doi:10.1136/adc.48.10.757 · Cited by 1,442

The later development of the brain and its vulnerability

Dobbing, J. (1982) · Journal of Inherited Metabolic Disease · doi:10.1007/bf01805569 · Cited by 391

Scientific Foundations of Paediatrics

Polani, P. E. (1974) · Archives of Disease in Childhood · doi:10.1136/adc.49.11.914-a · Cited by 290

Scientific Foundations of Paediatrics

Haworth, J. C. (1975) · JAMA · doi:10.1001/jama.1975.03240140055034 · Cited by 284

Vulnerability of Developing Brain. IX. The Effect of Nutritional Growth Retardation on the Timing of the Brain Growth-Spurt

Dobbing, J., & Sands, J. (2009) · Biology of the Neonate · doi:10.1159/000240430 · Cited by 275

Prenatal and postnatal growth and development of the central nervous system of the pig

Dickerson, J. W. T., & Dobbing, J. (1967) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1967.0002 · Cited by 269

Growth and development of the brain and spinal cord of the guinea pig

Dobbing, J., & Sands, J. (1970) · Brain Research · doi:10.1016/0006-8993(70)90311-2 · Cited by 244

Growth and Development of the Rabbit Brain

Harel, S., Watanabe, K. S., Linke, I., & Schain, R. J. (2009) · Biology of the Neonate · doi:10.1159/000240527 · Cited by 121

Fetal and Postnatal Cellular Growth

(1976) · Archives of Disease in Childhood · doi:10.1136/adc.51.6.487 · Cited by 77

A comparison of the albino rat with man in respect to the growth of the brain and of the spinal cord

Donaldson, H. H. (1908) · Journal of Comparative Neurology and Psychology · doi:10.1002/cne.920180402 · Cited by 69

Isoflurane exposure leads to apoptosis of neurons and oligodendrocytes in 20- and 40-day old rhesus macaques

Schenning, K. J., Noguchi, K. K., Martin, L. D., Manzella, F. M., Cabrera, O. H., Dissen, G. A., & Brambrink, A. M. (2016) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2016.11.006 · Cited by 81

Sevoflurane Acts on Ubiquitination–Proteasome Pathway to Reduce Postsynaptic Density 95 Protein Levels in Young Mice

Han, L., Liufu, N., Dong, Y., Xu, G., Zhang, Y., Shu, L., Soriano, S. G., Zheng, H., Yu, B., & Xie, Z. (2017) · Anesthesiology · doi:10.1097/aln.0000000000001889 · Cited by 81

Simvastatin Protects Against Long-Lasting Behavioral and Morphological Consequences of Neonatal Hypoxic/Ischemic Brain Injury

Balduini, W., Angelis, V. D., Mazzoni, E., & Cimino, M. (2001) · Stroke · doi:10.1161/hs0901.094287 · Cited by 81

Linoleic and α-linolenic acid as precursor and inhibitor for the synthesis of long-chain polyunsaturated fatty acids in liver and brain of growing pigs

Smink, W., Gerrits, W. J. J., Gloaguen, M., Ruiter, A., & van Baal, J. (2012) · animal · doi:10.1017/s1751731111001479 · Cited by 80

Transient activation of microglia following acute alcohol exposure in developing mouse neocortex is primarily driven by BAX-dependent neurodegeneration

Ahlers‐Dannen, K. E., Karaçay, B., Fuller, L. C., Bonthius, D. J., & Dailey, M. E. (2015) · Glia · doi:10.1002/glia.22835 · Cited by 85

Experimental model of pediatric asphyxial cardiopulmonary arrest in rats

Fink, E. L., Alexander, H. L., Marco, C. D., Dixon, C. E., Kochanek, P. M., Jenkins, L. W., Lai, Y., Donovan, H. A., Hickey, R. W., & Clark, R. S. B. (2004) · Pediatric Critical Care Medicine · doi:10.1097/01.pcc.0000112376.29903.8f · Cited by 80

The model of pentylenetetrazol-induced status epilepticus in the immature rat: short- and long-term effects

Nehlig, A., & de Vasconcelos, A. P. (1996) · Epilepsy Research · doi:10.1016/s0920-1211(96)00045-9 · Cited by 80

Multiple courses of antenatal steroids: risks and benefits

Walfisch, A. (2001) · Obstetrics and Gynecology · doi:10.1016/s0029-7844(01)01368-0 · Cited by 80

Photostimulation of brain lymphatics in male newborn and adult rodents for therapy of intraventricular hemorrhage

Li, D., Liu, S., Yu, T., Liu, Z., Sun, S., Bragin, D. E., Shirokov, A. A., Наволокин, Н. А., Bragina, O. A., Hu, Z., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-41710-y · Cited by 81

Differences in neonatal neurotoxicity of brominated flame retardants, PBDE 99 and TBBPA, in mice

Viberg, H., & Eriksson, P. (2011) · Toxicology · doi:10.1016/j.tox.2011.07.010 · Cited by 79

Effects of pre-natal alcohol exposure on hippocampal synaptic plasticity: Sex, age and methodological considerations

Fontaine, C. J., Patten, A. R., Sickmann, H. M., Helfer, J. L., & Christie, B. R. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.02.014 · Cited by 83

The importance of fetal/neonatal REM sleep

Mirmiran, M. (1986) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/0028-2243(86)90006-7 · Cited by 79

Astrocyte-synthesized oleic acid behaves as a neurotrophic factor for neurons

Medina, J. M., & Tabernero, A. (2002) · Journal of Physiology-Paris · doi:10.1016/s0928-4257(02)00015-3 · Cited by 79

Fetal Alcohol Spectrum Disorders and Neuroimmune Changes

Drew, P. D., & Kane, C. J. M. (2014) · International review of neurobiology · doi:10.1016/b978-0-12-801284-0.00003-8 · Cited by 82

Effects of low‐dose chlorpyrifos on neurobehavior and potential mechanisms: A review of studies in rodents, zebrafish, and Caenorhabditis elegans

Silva, M. H. (2020) · Birth Defects Research · doi:10.1002/bdr2.1661 · Cited by 81

17β‐estradiol protects against hypoxic/ischemic white matter damage in the neonatal rat brain

Gerstner, B., Lee, J., DeSilva, T. M., Jensen, F. E., Volpe, J. J., & Rosenberg, P. A. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22023 · Cited by 78

Prenatal Glucocorticoid Modifies Hypothalamo-Pituitary-Adrenal Regulation in Prepubertal Guinea Pigs

Dean, F., Yu, C., Lingas, R. I., & Matthews, S. G. (2001) · Neuroendocrinology · doi:10.1159/000054636 · Cited by 78

General Anesthetics in Pediatric Anesthesia: Influences on the Developing Brain

McCann, M. E., & Soriano, S. G. (2012) · Current Drug Targets · doi:10.2174/138945012800675768 · Cited by 77

Magnesium Is Not Consistently Neuroprotective for Perinatal Hypoxia-Ischemia in Term-Equivalent Models in Preclinical Studies: A Systematic Review

Galinsky, R., Bennet, L., Groenendaal, F., Lear, C. A., Tan, S., van Bel, F., Juul, S. E., Robertson, N. J., Mallard, C. E., & Gunn, A. J. (2014) · Developmental Neuroscience · doi:10.1159/000362206 · Cited by 77

Rapid NMDA receptor phosphorylation and oxidative stress precede striatal neurodegeneration after hypoxic ischemia in newborn piglets and are attenuated with hypothermia

Mueller‐Burke, D., Koehler, R. C., & Martin, L. J. (2007) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2007.08.015 · Cited by 77

A Neonatal Piglet Model for Investigating Brain and Cognitive Development in Small for Gestational Age Human Infants

Radlowski, E. C., Conrad, M. S., Lezmi, S., Dilger, R. N., Sutton, B. P., Larsen, R. J., & Johnson, R. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091951 · Cited by 77

Expression of orphanin FQ and the opioid receptor-like (ORL1) receptor in the developing human and rat brain

Neal, C. R., Akil, H., & Watson, S. J. (2002) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(01)00135-1 · Cited by 77

PKA-CREB-BDNF signaling pathway mediates propofol-induced long-term learning and memory impairment in hippocampus of rats

Zhong, Y., Chen, J., Li, L., Qin, Y., Wei, Y., Pan, S., Jiang, Y., Chen, J., & Xie, Y. (2018) · Brain Research · doi:10.1016/j.brainres.2018.04.022 · Cited by 77

Effects of a Period of Asphyxia during Birth on Spatial Learning in the Rat

Boksa, P., Krishnamurthy, A., & Brooks, W. (1995) · Pediatric Research · doi:10.1203/00006450-199504000-00018 · Cited by 77

Plasma and red blood cell fatty acid values as indexes of essential fatty acids in the developing organs of infants fed with milk or formulas

Innis, S. M. (1992) · The Journal of Pediatrics · doi:10.1016/s0022-3476(05)81240-5 · Cited by 77

Aberrant expression of miR‐218 and miR‐204 in human mesial temporal lobe epilepsy and hippocampal sclerosis—Convergence on axonal guidance

Kaalund, S. S., Venø, M. T., Bak, M., Møller, R. S., Laursen, H. B., Madsen, F., Broholm, H., Quistorff, B., Uldall, P. V., Tommerup, N., et al. (2014) · Epilepsia · doi:10.1111/epi.12839 · Cited by 76

Pro-Inflammatory Cytokine Regulation of P-glycoprotein in the Developing Blood-Brain Barrier

Iqbal, M., Ho, H. L., Sophie Petropoulos, A., Moisiadis, V. G., Gibb, W., & Matthews, S. G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043022 · Cited by 79

Congenital Viral Infections of the Brain: Lessons Learned from Lymphocytic Choriomeningitis Virus in the Neonatal Rat

Bonthius, D. J., & Perlman, S. M. (2007) · PLoS Pathogens · doi:10.1371/journal.ppat.0030149 · Cited by 76

The Serotonin Transporter and Early Life Stress: Translational Perspectives

Houwing, D. J., Buwalda, B., van der Zee, E. A., de Boer, S. F., & Olivier, J. D. A. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00117 · Cited by 83

Vasoactive intestinal peptide antagonist retards the development of neonatal behaviors in the rat

Hill, J. M., Gozes, I., Hill, J., Fridkin, M., & Brenneman, D. E. (1991) · Peptides · doi:10.1016/0196-9781(91)90186-s · Cited by 76

Anesthesia and the Developing Brain: A Review of Sevoflurane-induced Neurotoxicity in Pediatric Populations

Apai, C., Shah, R., Tran, K., & Shah, S. P. (2021) · Clinical Therapeutics · doi:10.1016/j.clinthera.2021.01.024 · Cited by 75

Blockade of the NLRP3/caspase-1 axis attenuates ketamine-induced hippocampus pyroptosis and cognitive impairment in neonatal rats

Zhang, Z., Bai, H., Ma, X., Shen, M., Li, R., Qiu, D., Li, S., & Gao, L. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02295-9 · Cited by 76

Memantine: Updating a rare success story in pro-cognitive therapeutics

Tari, P. K., Parsons, C. G., Collingridge, G. L., & Rammes, G. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109737 · Cited by 78

Iron Requirements in Infancy

Domellöf, M. (2011) · Annals of Nutrition and Metabolism · doi:10.1159/000332138 · Cited by 75

Docosapentaenoic acid does not completely replace DHA in n−3 FA‐deficient rats during early development

Greiner, R. S., Catalan, J. N., Moriguchi, T., & Salem, N. (2003) · Lipids · doi:10.1007/s11745-003-1080-2 · Cited by 75

The role of hypoxia-inducible transcription factors in the hypoxic neonatal brain

Trollmann, R., & Gassmann, M. (2009) · Brain and Development · doi:10.1016/j.braindev.2009.03.007 · Cited by 75

Protection with estradiol in developmental models of apoptotic neurodegeneration

Asimiadou, S., Bittigau, P., Felderhoff‐Mueser, U., Manthey, D., Sifringer, M., Pesditschek, S., Dzietko, M., Kaindl, A. M., Pytel, M., Studniarczyk, D., et al. (2005) · Annals of Neurology · doi:10.1002/ana.20553 · Cited by 75

Three-month nutritional supplementation in Indonesian infants and toddlers benefits memory function 8 y later

Pollitt, E., Watkins, W. E., & Husaini, M. (1997) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/66.6.1357 · Cited by 75

Cocaine acutely inhibits DNA synthesis in developing rat brain regions: evidence for direct actions

Anderson-Brown, T., Slotkin, T. A., & Seidler, F. J. (1990) · Brain Research · doi:10.1016/0006-8993(90)90358-i · Cited by 75

Prenatal disturbance alters the size of the corpus callosum in young monkeys

Coe, C. L., Lulbach, G. R., & Schneider, M. L. (2002) · Developmental Psychobiology · doi:10.1002/dev.10063 · Cited by 74

Neonatal alcohol and nicotine exposure limits brain growth and depletes cerebellar purkinje cells

Chen, W.-J. A., Parnell, S. E., & West, J. R. (1998) · Alcohol · doi:10.1016/s0741-8329(97)00084-0 · Cited by 74

Cryptic brain cell injury caused by fetal nicotine exposure is associated with persistent elevations of c-fos protooncogene expression1Supported by a grant from the Smokeles Tobacco Research Council.1

Slotkin, T. A., McCook, E. C., & Seidler, F. J. (1997) · Brain Research · doi:10.1016/s0006-8993(96)01345-5 · Cited by 74

Long-Term Effects of Neonatal Single or Multiple Isoflurane Exposures on Spatial Memory in Rats

Murphy, K. L., & Baxter, M. G. (2013) · Frontiers in Neurology · doi:10.3389/fneur.2013.00087 · Cited by 74

Ketamine and Neurotoxicity: Clinical Perspectives and Implications for Emergency Medicine

Green, S. M., & Coté, C. J. (2008) · Annals of Emergency Medicine · doi:10.1016/j.annemergmed.2008.10.003 · Cited by 74

Low doses of domoic acid during postnatal development produce permanent changes in rat behaviour and hippocampal morphology

Doucette, T. A., Bernard, P. B., Husum, H., Perry, M. A., Ryan, C. L., & Tasker, R. A. (2004) · Neurotoxicity Research · doi:10.1007/bf03033451 · Cited by 74

Mitochondrially targeted vitamin E and vitamin E mitigate ethanol-mediated effects on cerebellar granule cell antioxidant defense systems

Siler‐Marsiglio, K. I., Pan, Q., Paiva, M., Madorsky, I., Khurana, N. C., & Heaton, M. B. (2005) · Brain Research · doi:10.1016/j.brainres.2005.06.030 · Cited by 75

Consequences of early life MK-801 administration: Long-term behavioural effects and relevance to schizophrenia research

Lim, A. L., TAYLOR, D. A. H. B., & Malone, D. T. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.10.052 · Cited by 74

Expression of nitric oxide synthase isoforms and nitrotyrosine formation after hypoxia–ischemia in the neonatal rat brain

van den Tweel, E. R. W., Nijboer, C. H. A., Kavelaars, A., Heijnen, C. J., Groenendaal, F., & van Bel, F. (2005) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2005.06.031 · Cited by 74

Effects of Neonatal Antiepileptic Drug Exposure on Cognitive, Emotional, and Motor Function in Adult Rats

Forcelli, P. A., Kozlowski, R., Snyder, C., Kondratyev, A. D., & Gale, K. (2011) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.111.188862 · Cited by 74

Long-term Cognitive Impairments in Adult Rats Treated Neonatally with β-N-Methylamino-L-Alanine

Karlsson, O., Roman, E., & Brittebo, E. B. (2009) · Toxicological Sciences · doi:10.1093/toxsci/kfp196 · Cited by 74

Prenatal Binge-Like Alcohol Exposure in the Rat Results in Region-Specific Deficits in Brain Growth

Maier, S. E., Miller, J. A., & West, J. R. (1999) · Neurotoxicology and Teratology · doi:10.1016/s0892-0362(98)00056-7 · Cited by 74

Neonatal ethanol exposure: Functional alterations associated with cerebellar growth retardation

Meyer, L. S., Kotch, L. E., & Riley, E. P. (1990) · Neurotoxicology and Teratology · doi:10.1016/0892-0362(90)90107-n · Cited by 74

Long-term genomic and epigenomic dysregulation as a consequence of prenatal alcohol exposure: a model for fetal alcohol spectrum disorders

Kleiber, M. L., Chater‐Diehl, E., Laufer, B. I., Mantha, K., Chokroborty-Hoque, A., Alberry, B., & Singh, S. M. (2014) · Frontiers in Genetics · doi:10.3389/fgene.2014.00161 · Cited by 78

Fetal Learning About Ethanol and Later Ethanol Responsiveness: Evidence Against “Safe” Amounts of Prenatal Exposure

Abate, P., Pueta, M., Spear, N. E., & Molina, J. C. (2008) · Experimental Biology and Medicine · doi:10.3181/0703-mr-69 · Cited by 74

Infant maternal separation impairs adult cognitive performance in BALB/cJ mice

Wang, L., Jiao, J., & Dulawa, S. C. (2011) · Psychopharmacology · doi:10.1007/s00213-011-2209-4 · Cited by 80

Detection of Slipped-DNAs at the Trinucleotide Repeats of the Myotonic Dystrophy Type I Disease Locus in Patient Tissues

Axford, M. M., Wang, Y., Nakamori, M., Zannis‐Hadjopoulos, M., Thornton, C. A., & Pearson, C. E. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003866 · Cited by 73

Evaluation of a Long-Chain Polyunsaturated Fatty Acid Supplemented Formula on Growth, Tolerance, and Plasma Lipids in Preterm Infants up to 48 Weeks Postconceptional Age

Vanderhoof, J. A., Gross, S. J., Hegyi, T., Clandinin, T., Porcelli, P. J., DeCristofaro, J. D., Rhodes, T. T., Tsang, R. C., Shattuck, K. E., Cowett, R. M., et al. (1999) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1002/j.1536-4801.1999.tb02422.x · Cited by 73

Early Life Iron Deficiency Impairs Spatial Cognition in Neonatal Piglets ,2

Rytych, J. L., Elmore, M. R. P., Burton, M. D., Conrad, M. S., Donovan, S. M., Dilger, R. N., & Johnson, R. W. (2012) · Journal of Nutrition · doi:10.3945/jn.112.165522 · Cited by 79

The Domestic Piglet: An Important Model for Investigating the Neurodevelopmental Consequences of Early Life Insults

Conrad, M. S., & Johnson, R. W. (2014) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-022114-111049 · Cited by 79

Phosphorylation of Microtubule Proteins in Rat Brain at Different Developmental Stages: Comparison with That Found in Neuronal Cultures

Díaz‐Nido, J., Serrano, L., Hernandez, M. A., & Ávila, J. (1990) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1990.tb13303.x · Cited by 73

Transgenerational effects of prenatal synthetic glucocorticoids on hypothalamic-pituitary-adrenal function

Iqbal, M., Moisiadis, V. G., Kostaki, A., & Matthews, S. G. (2012) · Endocrinology · doi:10.1210/en.2012-1054 · Cited by 72

Impact of fetal nicotine exposure on development of rat brain regions: critical sensitive periods or effects of withdrawal?

Slotkin, T. A., Lappi, S. E., & Seidler, F. J. (1993) · Brain Research Bulletin · doi:10.1016/0361-9230(93)90224-y · Cited by 72

Early Exposure to Alcohol Leads to Permanent Impairment of Dendritic Excitability in Neocortical Pyramidal Neurons

Granato, A., Palmer, L. M., Giorgio, A. D., Tavian, D., & Larkum, M. E. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5520-11.2012 · Cited by 72

Low-level lead exposure triggers neuronal apoptosis in the developing mouse brain

Dribben, W. H., Creeley, C. E., & Farber, N. B. (2011) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2011.05.006 · Cited by 74

Anesthesia-Induced Neurodegeneration in Fetal Rat Brains

Wang, S., Peretich, K., Zhao, Y., Liang, G., Meng, Q., & Wei, H. (2009) · Pediatric Research · doi:10.1203/pdr.0b013e3181b3381b · Cited by 72

The Effect of Chlorpyrifos and Chlorpyrifos-Oxon on Brain Cholinesterase, Muscarinic Receptor Binding, and Neurotrophin Levels in Rats Following Early Postnatal Exposure

Betancourt, A. M. (2003) · Toxicological Sciences · doi:10.1093/toxsci/kfh003 · Cited by 72

Delayed growth, motor function and learning in preterm pigs during early postnatal life

Andersen, A. D., Sangild, P. T., Munch, S. L., van der Beek, E. M., Renes, I. B., Ginneken, C. J. V., Greisen, G. O., & Thymann, T. (2016) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00349.2015 · Cited by 72

Neonatal binge alcohol exposure increases microglial activation in the developing rat hippocampus

Boschen, K. E., Ruggiero, M., & Klintsova, A. Y. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.03.033 · Cited by 72

Developmental neurotoxic effects of two pesticides: Behavior and neuroprotein studies on endosulfan and cypermethrin

Lee, I., Eriksson, P., Fredriksson, A., Buratovic, S., & Viberg, H. (2015) · Toxicology · doi:10.1016/j.tox.2015.06.010 · Cited by 75

Long-Chain Polyunsaturated Fatty Acid Levels in Formulae Influence Deposition of Docosahexaenoic Acid and Arachidonic Acid in Brain and Red Blood Cells of Artificially Reared Neonatal Rats

Ward, G. R., Huang, Y. S., BOBIK, E. G., Xing, H. C., Mutsaers, L., Auestad, N., Montalto, M., & Wainwright, P. E. (1998) · Journal of Nutrition · doi:10.1093/jn/128.12.2473 · Cited by 72

Maturation-dependent oligodendrocyte apoptosis caused by hyperoxia

Gerstner, B., Bührer, C., Rheinländer, C., Polley, O., Schüller, A., Berns, M., Obladen, M., & Felderhoff‐Mueser, U. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.20880 · Cited by 72

Heme Regulation in Traumatic Brain Injury: Relevance to the Adult and Developing Brain

Chang, E. F., Claus, C. P., Vreman, H. J., Wong, R. J., & Noble‐Haeusslein, L. J. (2005) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600147 · Cited by 72

Psychomotor functions in developing rats: Ontogenetic approach to structure-function relationships

Bâ, A. (1995) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(94)00042-y · Cited by 72

Early exposure to nicotine during critical periods of brain development: mechanisms and consequences

Smith, A., Dwoskin, L., & Pauly, J. (2016) · Journal of Pediatric Biochemistry · doi:10.1055/s-0036-1586367 · Cited by 71

Antenatal Glucocorticoid Treatment Affects Hippocampal Development in Mice

Noorlander, C. W., Tijsseling, D., Hessel, E. V. S., de Vries, W. B., Derks, J. B., Visser, G. H. A., & Graan, P. N. E. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085671 · Cited by 77

Postnatal environmental or experiential amelioration of neurobehavioral effects of perinatal alcohol exposure in rats

Hannigan, J. H., O’Leary‐Moore, S. K., & Berman, R. F. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.06.019 · Cited by 71

Low brain glutathione and ascorbic acid associated with dopamine uptake inhibition during rat's development induce long-term cognitive deficit: relevance to schizophrenia

Castagné, V., Rougemont, M., Cuénod, M., & Kim, Q. (2003) · Neurobiology of Disease · doi:10.1016/j.nbd.2003.09.005 · Cited by 71

Prenatal activation of Toll-like receptors-3 by administration of the viral mimetic poly(I:C) changes synaptic proteins, N-methyl-D-aspartate receptors and neurogenesis markers in offspring

Forrest, C. M., Khalil, O. S., Pisar, M., Smith, R. A., Darlington, L. G., & Stone, T. W. (2012) · Molecular Brain · doi:10.1186/1756-6606-5-22 · Cited by 72

Autophagy activation involved in hypoxic‐ischemic brain injury induces cognitive and memory impairment in neonatal rats

Xu, Y., Tian, Y., Tian, Y., Li, X., & Zhao, P. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13851 · Cited by 71

Infant Rat Model of the Shaken Baby Syndrome: Preliminary Characterization and Evidence for the Role of Free Radicals in Cortical Hemorrhaging and Progressive Neuronal Degeneration

SMITH, S. L., Andrus, P. K., Gleason, D. D., & Hall, E. D. (1998) · Journal of Neurotrauma · doi:10.1089/neu.1998.15.693 · Cited by 71

Docosahexaenoic acid in developing brain and retina of piglets fed high or low α‐linolenate formula with and without fish oil

Arbuckle, L. D., & Innis, S. M. (1992) · Lipids · doi:10.1007/bf02535805 · Cited by 71

The challenge of understanding cerebral white matter injury in the premature infant

Elitt, C. M., & Rosenberg, P. A. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.04.038 · Cited by 70

Effects of Perinatal Exposure to Ketamine on the Developing Brain

Cheung, H. M., & Yew, D. T. W. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00138 · Cited by 70

General anesthetic-induced neurotoxicity: an emerging problem for the young and old?

Culley, D. J., Xie, Z., & Crosby, G. J. (2007) · Current Opinion in Anaesthesiology · doi:10.1097/aco.0b013e3282efd18b · Cited by 70

GABAA Receptors, Anesthetics and Anticonvulsants in Brain Development

Henschel, O., Gipson, K. E., & Bordey, A. (2008) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/187152708784083812 · Cited by 70

Glutamate signaling and the fetal alcohol syndrome

Olney, J. W., Wozniak, D. F., Jevtović‐Todorović, V., & Ikonomidou, C. (2001) · Mental Retardation and Developmental Disabilities Research Reviews · doi:10.1002/mrdd.1037 · Cited by 70

Developmental changes in the sensitivity of the neonatal rat brain to hypoxic/ischemic injury

Grafe, M. R. (1994) · Brain Research · doi:10.1016/0006-8993(94)90385-9 · Cited by 70

Effects of chronic prenatal ethanol exposure on locomotor activity, and hippocampal weight, neurons, and nitric oxide synthase activity of the young postnatal guinea pig

Gibson, M., Butters, N. S., Reynolds, J. N., & Brien, J. F. (2000) · Neurotoxicology and Teratology · doi:10.1016/s0892-0362(99)00074-4 · Cited by 70

Response of (n-3) and (n-6) Fatty Acids in Piglet Brain, Liver and Plasma to Increasing, but Low, Fish Oil Supplementation of Formula

Arbuckle, L. D., Rioux, F. M., Mackinnon, M., Hrboticky, N., & Innis, S. M. (1991) · Journal of Nutrition · doi:10.1093/jn/121.10.1536 · Cited by 70

Late emerging effects of prenatal and early postnatal nicotine exposure on the cholinergic system and anxiety-like behavior

Eppolito, A. K., Bachus, S. E., McDonald, C. G., Meador-Woodruff, J. H., & Smith, R. F. (2010) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2009.12.009 · Cited by 69

Hypoxic‐ischemic‐related cerebrovascular changes and potential therapeutic strategies in the neonatal brain

Disdier, C., & Stonestreet, B. S. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24590 · Cited by 72

Mechanism and Developmental Changes in Iron Transport across the Blood-Brain Barrier

Morgan, E. H., & Moos, T. (2002) · Developmental Neuroscience · doi:10.1159/000065699 · Cited by 69

A single neonatal exposure to perfluorohexane sulfonate (PFHxS) affects the levels of important neuroproteins in the developing mouse brain

Lee, I., & Viberg, H. (2013) · NeuroToxicology · doi:10.1016/j.neuro.2013.05.007 · Cited by 70

Bacterial infection early in life protects against stressor-induced depressive-like symptoms in adult rats

Bilbo, S. D., Yirmiya, R., Amat, J., Paul, E. D., Watkins, L. R., & Maier, S. F. (2008) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2007.11.008 · Cited by 75

Drugs of abuse that cause developing neurons to commit suicide

Farber, N. B., & Olney, J. W. (2003) · Developmental Brain Research · doi:10.1016/j.devbrainres.2003.09.009 · Cited by 69

Prolonged maternal separation disturbs the serotonergic system during early brain development

Ohta, K., Miki, T., Warita, K., Suzuki, S., Kusaka, T., Yakura, T., Liu, J., Tamai, M., & Takeuchi, Y. (2014) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2013.10.007 · Cited by 68

Minimal variation in eutherian brain growth rates during fetal neurogenesis

Halley, A. C. (2017) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2017.0219 · Cited by 68

Caffeine protects neuronal cells against injury caused by hyperoxia in the immature brain

Endesfelder, S., Zaak, I., Weichelt, U., Bührer, C., & Schmitz, T. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.09.026 · Cited by 68

Neurodevelopmental consequences of maternal distress: what do we really know?

Schuurmans, C., & Kurrasch, D. M. (2012) · Clinical Genetics · doi:10.1111/cge.12049 · Cited by 69

Resuscitation with supplementary oxygen induces oxidative injury in the cerebral cortex

Solberg, R., Longini, M., Proietti, F., Vezzosi, P., Saugstad, O. D., & Buonocore, G. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.07.022 · Cited by 67

Duration of fetoscopic spina bifida repair does not affect the central nervous system in fetal lambs

Vergote, S., Joyeux, L., Basurto, D., Bleeser, T., Valenzuela, I. J., Valentyn, B., Emam, D., Watananirun, K., Bie, F. R. D., Aertsen, M., et al. (2023) · American Journal of Obstetrics & Gynecology MFM · doi:10.1016/j.ajogmf.2023.101156 · Cited by 3

43 Adding fetal surgery to general anesthesia does not impair brain development in the rabbit model

der Veeken, L. V., Emam, D., Bleeser, T., Valenzuela, I. J., Rex, S., & Deprest, J. A. (2021) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2020.12.119

Longitudinal evolution of central nervous system anomalies in fetuses with open spina bifida fetoscopic repair and correlation with neurologic outcome

Trigo, L., Eixarch, E., Faig, F., Gómez‐Chiari, M., Rebollo, M., Dalaqua, M., Gratacós, E., & Lapa, D. (2023) · American Journal of Obstetrics & Gynecology MFM · doi:10.1016/j.ajogmf.2023.100932 · Cited by 10

Neuroprotection is improved by watertightness of fetal spina bifida repair in the sheep model

Joyeux, L., van der Merwe, J., Aertsen, M., Patel, P. A., Khatoun, A., da Cunha, M. G. M. C. M., Vleeschauwer, S. D., Parra, J., Danzer, E., Laughlin, M. M., et al. (2022) · Ultrasound in Obstetrics and Gynecology · doi:10.1002/uog.24907 · Cited by 14

Safety and efficacy of fetal surgery techniques to close a spina bifida defect in the fetal lamb model: A systematic review

Joyeux, L., Bie, F. R. D., Danzer, E., Mieghem, T. V., Flake, A. W., & Deprest, J. A. (2018) · Prenatal Diagnosis · doi:10.1002/pd.5222 · Cited by 27